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Genome Med
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome
- M.N. Bainbridge
- H. Hu
- D.M. Muzny
- L. Musante
- J.R. Lupski
- B.H. Graham
- W. Chen
- K.W. Gripp
- K. Jenny
- T.F. Wienker
- Y. Yang
- V.R. Sutton
- R.A. Gibbs
- H.H. Ropers